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A Diels-Alder approach for the synthesis of highly functionalized benzo-annulated indane-based α-amino acid derivatives via a sultine intermediate

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Title A Diels-Alder approach for the synthesis of highly functionalized benzo-annulated indane-based α-amino acid derivatives via a sultine intermediate
 
Creator KOTHA, SAMBASIVARAO
GHOSH, ARUN KUMAR
 
Subject cycloaddition
amino acids
derivatives
synthesis
 
Description The synthesis of various highly functionalized benzo-annulated indane-based α-amino acid (AAA) derivatives are reported via a [4+2] cycloaddition strategy using a sultine derivative, containing an AAA moiety, as a reactive diene component. By adopting this strategy, a new α,α-dialkylated indane-based C60 fullerene containing a constrained AAA unit is reported.
 
Publisher Elsevier
 
Date 2009-02-26T06:04:45Z
2011-11-25T17:29:59Z
2011-12-26T13:06:24Z
2011-12-27T05:54:14Z
2009-02-26T06:04:45Z
2011-11-25T17:29:59Z
2011-12-26T13:06:24Z
2011-12-27T05:54:14Z
2004
 
Type Article
 
Identifier Tetrahedron Letters 45(14), 2931-2934
0040-4039
http://dx.doi.org/10.1016/j.tetlet.2004.02.060
http://hdl.handle.net/10054/787
http://dspace.library.iitb.ac.in/xmlui/handle/10054/787
 
Language en